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Terminated

ADP2.1 Adapter, non-sterile reusable Model Number: 30-802-1 ,an accessory used with the TissueLink BiPolar Floating Device

FDA Recall Z-1415-04 · Posted 2004-09-01

Recalling FirmTissueLink Medical, Inc.
Recall StatusTerminated
Product CodeGEI
Date Initiated2004-07-22
Date Terminated2004-10-04
Product Quantity164 units

Reason for Recall

Adapter when connected to a generator may short circuit resulting in lack of power and/or thermal warming of the ADP housing.

Firm Action

TissueLink notified the sales force on 7/22/04 to visit each account and retreive product at the hospital level.

Root Cause

Other

Distribution Pattern

Nationwide

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K022532TISSUELINK BIPOLAR FLOATING BALL DEVICETissuelink Medical, Inc. · 2003-02-12K020574TISSUELINK BIPOLAR FLOATING BALL DEVICETissuelink Medical, Inc. · 2002-05-20

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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